Canonical Allele Identifier: CA1941460032
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462097G= , CM000672.2:g.122462097G= GRCh38
NC_000010.10:g.124221613G= , CM000672.1:g.124221613G= GRCh37
NC_000010.9:g.124211603G= NCBI36
NG_011554.1:g.5573G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.445G= MANE Select ENSP00000357980.3:p.Val149=
ENST00000648167.1:c.154+3388G= ENSP00000498033.1:n.154+3388G=
ENST00000368984.7:c.445G= ENSP00000357980.3:p.Val149=
NM_002775.4:c.445G= NP_002766.1:p.Val149=
NM_002775.5:c.445G= MANE Select NP_002766.1:p.Val149=
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